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Parkinsonism & Related Disorders|February 28, 2020
The impact of ethnicity on the clinical presentations of spinocerebellar ataxia type 3Shi-Rui Gan, Karla P Figueroa, Hao-Ling Xu, et al.Cancer Research|August 15, 2008
Variants in the ATM gene associated with a reduced risk of contralateral breast cancerPatrick Concannon, Robert W Haile, Anne-Lise Børresen-Dale, et al.Frontiers in Molecular Biosciences|September 22, 2022
A non-synonymous single nucleotide polymorphism in SIRT6 predicts neurological severity in Friedreich ataxiaLayne N Rodden, Christian Rummey, Yi Na Dong, et al.Breast Cancer Research : BCR|April 16, 2004
Study design: evaluating gene-environment interactions in the etiology of breast cancer - the WECARE studyJonine L Bernstein, Bryan Langholz, Robert W Haile, et al.Parkinsonism & Related Disorders|November 2, 2017
Dystonia and ataxia progression in spinocerebellar ataxiasPei-Hsin Kuo, Shi-Rui Gan, Jie Wang, et al.Journal of the Neurological Sciences|May 27, 2020
Dysphagia in spinocerebellar ataxias type 1, 2, 3 and 6Chen-Ya Yang, Ruo-Yah Lai, Nadia Amokrane, et al.Journal of the National Cancer Institute|March 23, 2010
Radiation exposure, the ATM Gene, and contralateral breast cancer in the women's environmental cancer and radiation epidemiology studyJonine L Bernstein, Robert W Haile, Marilyn Stovall, et al.The Lancet. Neurology|August 16, 2024
Safety and efficacy of intra-erythrocyte dexamethasone sodium phosphate in children with ataxia telangiectasia (ATTeST): a multicentre, randomised, double-blind, placebo-controlled phase 3 trialStefan Zielen, Thomas Crawford, Luca Benatti, et al.Human Mutation|October 15, 2013
Extreme growth failure is a common presentation of ligase IV deficiencyJennie E Murray, Louise S Bicknell, Gökhan Yigit, et al.Human Mutation|November 7, 2019
A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disordersKathie J Ngo, Jessica E Rexach, Hane Lee, et al.Pageof 19